LT3311B - Aqueous coating composition and process for manufacture thereof - Google Patents
Aqueous coating composition and process for manufacture thereof Download PDFInfo
- Publication number
- LT3311B LT3311B LTIP527A LTIP527A LT3311B LT 3311 B LT3311 B LT 3311B LT IP527 A LTIP527 A LT IP527A LT IP527 A LTIP527 A LT IP527A LT 3311 B LT3311 B LT 3311B
- Authority
- LT
- Lithuania
- Prior art keywords
- weight
- coating
- acid
- monomers
- epoxy resin
- Prior art date
Links
- 239000008199 coating composition Substances 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 17
- 230000008569 process Effects 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000002253 acid Substances 0.000 claims description 45
- 238000000576 coating method Methods 0.000 claims description 45
- 239000011248 coating agent Substances 0.000 claims description 41
- 239000000178 monomer Substances 0.000 claims description 38
- 239000000203 mixture Substances 0.000 claims description 37
- 239000003822 epoxy resin Substances 0.000 claims description 31
- 229920000647 polyepoxide Polymers 0.000 claims description 31
- 239000003999 initiator Substances 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- 239000011230 binding agent Substances 0.000 claims description 19
- -1 glycidyl ester Chemical class 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 150000007513 acids Chemical class 0.000 claims description 13
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- 230000003472 neutralizing effect Effects 0.000 claims description 11
- 150000002978 peroxides Chemical class 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 239000003960 organic solvent Substances 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000049 pigment Substances 0.000 claims description 6
- 238000010526 radical polymerization reaction Methods 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 125000003700 epoxy group Chemical group 0.000 claims description 5
- 229920002521 macromolecule Polymers 0.000 claims description 5
- 239000004033 plastic Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 4
- 238000005886 esterification reaction Methods 0.000 claims description 4
- 125000000466 oxiranyl group Chemical group 0.000 claims description 4
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 230000032050 esterification Effects 0.000 claims description 3
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 229960002887 deanol Drugs 0.000 claims description 2
- 239000012972 dimethylethanolamine Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 230000001476 alcoholic effect Effects 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000006185 dispersion Substances 0.000 description 24
- 239000004922 lacquer Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 18
- 235000013361 beverage Nutrition 0.000 description 17
- 239000002966 varnish Substances 0.000 description 15
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 13
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 12
- 238000009713 electroplating Methods 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 11
- 238000007654 immersion Methods 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 10
- 239000000047 product Substances 0.000 description 9
- 239000004593 Epoxy Substances 0.000 description 8
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 229920001568 phenolic resin Polymers 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- 150000008065 acid anhydrides Chemical class 0.000 description 5
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 230000001954 sterilising effect Effects 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 150000002605 large molecules Chemical class 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 description 1
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- IEVADDDOVGMCSI-UHFFFAOYSA-N 2-hydroxybutyl 2-methylprop-2-enoate Chemical compound CCC(O)COC(=O)C(C)=C IEVADDDOVGMCSI-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- RDFQSFOGKVZWKF-UHFFFAOYSA-N 3-hydroxy-2,2-dimethylpropanoic acid Chemical compound OCC(C)(C)C(O)=O RDFQSFOGKVZWKF-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 1
- OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 229920003270 Cymel® Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical group CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- KQNZLOUWXSAZGD-UHFFFAOYSA-N benzylperoxymethylbenzene Chemical compound C=1C=CC=CC=1COOCC1=CC=CC=C1 KQNZLOUWXSAZGD-UHFFFAOYSA-N 0.000 description 1
- 235000012206 bottled water Nutrition 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- RLGKNOKKEQLVIU-UHFFFAOYSA-N ethanol Chemical compound CCO.CCO.CCO.CCO RLGKNOKKEQLVIU-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical class O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000004801 process automation Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical group C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/10—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers containing more than one epoxy radical per molecule
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Pens And Brushes (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19863627860 DE3627860A1 (de) | 1986-08-16 | 1986-08-16 | Waessriges ueberzugsmittel, verfahren zu seiner herstellung sowie seine verwendung zur beschichtung von dosen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| LTIP527A LTIP527A (en) | 1994-11-25 |
| LT3311B true LT3311B (en) | 1995-06-26 |
Family
ID=6307558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LTIP527A LT3311B (en) | 1986-08-16 | 1993-05-06 | Aqueous coating composition and process for manufacture thereof |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US4997865A (de) |
| EP (2) | EP0324741A1 (de) |
| JP (1) | JP2536889B2 (de) |
| CN (1) | CN1012069B (de) |
| AT (1) | ATE58389T1 (de) |
| AU (1) | AU607934B2 (de) |
| BR (1) | BR8707772A (de) |
| CA (1) | CA1306566C (de) |
| DE (2) | DE3627860A1 (de) |
| DK (1) | DK172740B1 (de) |
| ES (1) | ES2018670B3 (de) |
| FI (1) | FI97065C (de) |
| GR (1) | GR3002551T3 (de) |
| IE (1) | IE60579B1 (de) |
| LT (1) | LT3311B (de) |
| LV (1) | LV10473B (de) |
| MD (1) | MD940049A (de) |
| NO (1) | NO300811B1 (de) |
| NZ (1) | NZ221445A (de) |
| PT (1) | PT85541B (de) |
| RU (1) | RU2074210C1 (de) |
| WO (1) | WO1988001287A1 (de) |
| ZA (1) | ZA876028B (de) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4001251A1 (de) * | 1990-01-18 | 1991-07-25 | Basf Lacke & Farben | Beschichtungsmasse, verfahren zu ihrer herstellung sowie deren verwendung |
| DE4010167C2 (de) * | 1990-03-30 | 1996-04-11 | Basf Lacke & Farben | Verfahren zur Innenbeschichtung von Blechemballagen, Beschichtungsmittel auf Basis eines carboxylgruppenhaltigen Polyesters und eines Phenols und dessen Verwendung |
| DE4019030A1 (de) * | 1990-06-14 | 1991-12-19 | Herberts Gmbh | Wasserverduennbare bindemittel auf epoxidharzbasis, verfahren zu deren herstellung und deren verwendung fuer waessrige ueberzugsmittel, sowie waessrige ueberzugsmittel |
| DE4132083A1 (de) * | 1991-09-26 | 1993-04-01 | Basf Lacke & Farben | Verfahren zur elektrophoretischen innenbeschichtung von metallbehaeltern zur aufbewahrung von lebensmitteln und getraenken |
| JP2921188B2 (ja) * | 1991-07-19 | 1999-07-19 | 東洋インキ製造株式会社 | 無硬化触媒型水性塗料 |
| DE4131706C2 (de) * | 1991-09-24 | 1994-10-20 | Basf Lacke & Farben | Verfahren zur Herstellung einer wäßrigen Beschichtungszusammensetzung, wäßrige Beschichtungszusammensetzungen sowie deren Verwendung zur Beschichtung von Emballagen |
| US5354366A (en) * | 1993-09-27 | 1994-10-11 | Deluxe Corporation | Ink composition and resins and methods relating thereto |
| EP0769508B1 (de) * | 1994-07-07 | 2001-10-17 | Nippon Paint Co., Ltd. | Wasserdispergierbare harzzusammensetzung und verfahren zur herstellung derselben |
| DE19625774A1 (de) * | 1996-06-27 | 1998-01-02 | Hoechst Ag | Selbstvernetzende wäßrige Dispersionen von Polyestern und Vinylpolymeren |
| DE19637970A1 (de) | 1996-09-18 | 1998-03-19 | Basf Lacke & Farben | Beschichtungsmittel, Verfahren zu seiner Herstellung sowie die Verwendung des Beschichtungsmittels, insbesondere zur Außenlackierung von Emballagen |
| DE19714015A1 (de) * | 1997-04-04 | 1998-10-08 | Basf Ag | Lösungen von Aminotriazinharzen in Monoalkyloglycolen |
| US6180726B1 (en) | 1998-03-10 | 2001-01-30 | H. B. Fuller Licensing & Financing Inc. | High temperature resistant coating composition and method of using thereof |
| RU2220994C1 (ru) * | 1998-03-17 | 2004-01-10 | Бп Корпорейшн Норт Америка Инк. | Эпоксиаминоакрилатная эмульсия на водной основе и полученное с ее использованием облицовочное покрытие контейнера |
| US6494983B1 (en) * | 1998-11-19 | 2002-12-17 | White Cap, Inc. | Composition and method for promoting adhesion of thermoplastic elastomers to metal substrates |
| US6214188B1 (en) * | 1998-12-21 | 2001-04-10 | Basf Corporation | Anodic electrocoat having a carbamate functional resin |
| PL199178B1 (pl) * | 1999-04-21 | 2008-08-29 | Ppg Ind Lacke Gmbh | Polimerowe mikrocząstki i ich zastosowanie |
| US6190523B1 (en) * | 1999-07-20 | 2001-02-20 | Basf Corporation | Electrocoat coating composition and process for electrocoating a substrate |
| US6423774B1 (en) * | 2000-03-21 | 2002-07-23 | Ppg Industries Ohio, Inc. | Cationic aliphatic polyester resins and their electrodeposition |
| KR20020080034A (ko) * | 2001-04-10 | 2002-10-23 | 삼화페인트공업주식회사 | 식관 내면용 아크릴 변성 수용성 에폭시수지 조성물 및 그제조방법 |
| WO2003057770A1 (en) * | 2001-12-31 | 2003-07-17 | Advanced Cardiovascular Systems, Inc. | Porous polymer articles and methods of making the same |
| KR100496048B1 (ko) * | 2001-12-31 | 2005-06-17 | 주식회사 디피아이 | 아크릭 변성 폴리에스테르 조성물 |
| CN100412114C (zh) * | 2003-04-02 | 2008-08-20 | 瓦尔斯帕供应公司 | 水性分散体和涂料 |
| DE10345788A1 (de) * | 2003-10-02 | 2005-04-21 | Bayer Materialscience Ag | Wässrige Beschichtungsmittel für Can Coating |
| ES2367516T3 (es) * | 2004-10-20 | 2011-11-04 | Valspar Sourcing, Inc. | Composiciones de recubrimiento para latas y métodos de recubrimiento. |
| ES2525408T3 (es) * | 2004-12-22 | 2014-12-22 | Akzo Nobel Coatings International B.V. | Dispersiones poliméricas acuosas |
| KR100609771B1 (ko) | 2004-12-31 | 2006-08-08 | 주식회사 케이씨씨 | 포름알데히드를 함유하지 않는 수용성 아크릴 수지 및이를 함유하는 유리면 바인더 조성물 |
| US20070080065A1 (en) * | 2005-10-07 | 2007-04-12 | Jeffrey Oravitz | Methods for electrocoating full panel easy open ends |
| CA2622550C (en) * | 2005-10-18 | 2014-03-25 | Valspar Sourcing, Inc. | Coating compositions for containers and methods of coating |
| US8361301B2 (en) * | 2009-03-31 | 2013-01-29 | Ppg Industries Ohio, Inc. | Electrocoating composition comprising a crater control additive |
| CN102387924B (zh) | 2009-04-09 | 2014-10-15 | 威士伯采购公司 | 具有不饱和脂环官能团的聚合物以及由其形成的涂料组合物 |
| US8486574B2 (en) * | 2009-07-14 | 2013-07-16 | Ford Global Technologies, Llc | Method and system for power control in an automotive vehicle |
| US8754614B2 (en) * | 2009-07-17 | 2014-06-17 | Tesla Motors, Inc. | Fast charging of battery using adjustable voltage control |
| WO2011009040A1 (en) | 2009-07-17 | 2011-01-20 | Valspar Sourcing, Inc. | Coating composition and articles coated therewith |
| AU2010295405B2 (en) | 2009-09-18 | 2015-09-24 | Swimc Llc | Polyurethane coating composition |
| MY183896A (en) * | 2010-03-26 | 2021-03-17 | Nippon Paint Co Ltd | Water-based coating composition, and process for formation of coating film and process for formation of multilayer coating film, which comprise using the water-based coating compostion |
| CN102140299B (zh) * | 2011-04-08 | 2013-04-17 | 广州慧谷化学有限公司 | 一种具有自润滑功能的适合高速冲制的易拉罐罐盖涂料 |
| US9752044B2 (en) * | 2013-08-16 | 2017-09-05 | Ppg Industries Ohio, Inc. | Aqueous-based coating composition containing an oleoresinous component |
| WO2013158261A1 (en) * | 2012-04-18 | 2013-10-24 | Valspar Corporation | Low voc, water-based coating compositions suitable for protecting metal containing substrates including food and beverage packages |
| CN102977338B (zh) * | 2012-11-08 | 2015-08-26 | 西安交通大学 | 一种水性环氧树脂及其制备方法及制备清漆的方法 |
| JP6191221B2 (ja) * | 2013-04-25 | 2017-09-06 | 凸版印刷株式会社 | 水系コーティング剤およびガスバリア性フィルム |
| US20150017359A1 (en) * | 2013-07-11 | 2015-01-15 | Ppg Industries Ohio, Inc. | Coating compositions with improved adhesion to containers |
| EP3242907B1 (de) * | 2015-01-05 | 2020-12-02 | Rhodia Operations | Amine-imino-dialkohol-neutralisierungsmittel für wässrige organische beschichtungszusammensetzungen mit geringem anteil an flüchtigen verbindungen und verfahren zur verwendung davon |
| JP7232022B2 (ja) * | 2018-04-13 | 2023-03-02 | 東洋インキＳｃホールディングス株式会社 | 水性塗料組成物、缶用部材、及び缶 |
| WO2019198810A1 (ja) * | 2018-04-13 | 2019-10-17 | 東洋インキＳｃホールディングス株式会社 | 水性塗料組成物、缶用部材、及び缶 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3862914A (en) | 1972-11-01 | 1975-01-28 | Mobil Oil Corp | Water-based coatings from polyepoxides and polycarboxylic acid monoanhydrides |
| US3960795A (en) | 1974-08-13 | 1976-06-01 | Ppg Industries, Inc. | Hydrolyzed reaction product of a polyepoxide with a phenolic compound having a group hydrolyzable to carboxyl |
| EP0006334A1 (de) | 1978-06-12 | 1980-01-09 | Mobil Oil Corporation | Verfahren zur Herstellung von selbstemulgierbaren Epoxyharzester-Copolymeren und die so hergestellten Produkte |
| EP0006336A1 (de) | 1978-06-12 | 1980-01-09 | Mobil Oil Corporation | Überzugsmittel aus wässrigen Emulsionen auf der Basis von selbstemulgierbaren veresterten Polyepoxyden-Copolymeren Zusammensetzungen |
| US4212781A (en) | 1977-04-18 | 1980-07-15 | Scm Corporation | Modified epoxy resins, processes for making and using same and substrates coated therewith |
| US4247439A (en) | 1973-11-06 | 1981-01-27 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from epoxy resin, polymeric acid and tertiary amine |
| US4308185A (en) | 1976-05-11 | 1981-12-29 | Scm Corporation | Graft polymer compositions of terminated epoxy resin, processes for making and using same, and substrates coated therewith |
| DE3446178A1 (de) | 1983-12-21 | 1985-07-04 | Inmont Corp., Clifton, N.J. | Wasserverduennbare anstrichzusammensetzung, verfahren zu ihrer herstellung und ihre verwendung zum beschichten von behaeltern fuer nahrungsmittel |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2608901A1 (de) * | 1976-03-04 | 1977-09-08 | Hoechst Ag | Verfahren zur herstellung von haertbaren, fluessigen, epoxidgruppen enthaltenden pfropfcopolymerisaten |
| DE2608869A1 (de) * | 1976-03-04 | 1977-09-08 | Hoechst Ag | Verfahren zur herstellung von haertbaren, fluessigen, epoxidgruppen enthaltenden pfropfcopolymerisaten |
| JPS54102399A (en) * | 1978-01-30 | 1979-08-11 | Hitachi Chem Co Ltd | Preparation of water-thinnable resin |
| US4302373A (en) * | 1980-08-05 | 1981-11-24 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from modified epoxy resin, polymeric acid and tertiary amine |
| US4423165A (en) * | 1982-04-16 | 1983-12-27 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from epoxy resin, first polymeric acid, tertiary amine and second polymeric acid |
| JPS58180521A (ja) * | 1982-04-16 | 1983-10-22 | Asahi Chem Ind Co Ltd | 可撓性エポキシ樹脂の製造方法 |
| JPS5951909A (ja) * | 1982-09-20 | 1984-03-26 | Toyo Ink Mfg Co Ltd | 水性樹脂分散体組成物 |
| US4476262A (en) * | 1982-12-30 | 1984-10-09 | Mobil Oil Corporation | Aqueous coatings comprising ionic polymer ester and diluent polymer with reduced monomer residue and method of preparation |
| US4444923A (en) * | 1982-12-30 | 1984-04-24 | Mobil Oil Corporation | Process for preparing aqueous coatings comprising dispersible epoxy resin-acid polymer ester |
-
1986
- 1986-08-16 DE DE19863627860 patent/DE3627860A1/de not_active Withdrawn
-
1987
- 1987-08-13 US US07/327,964 patent/US4997865A/en not_active Expired - Fee Related
- 1987-08-13 AU AU77888/87A patent/AU607934B2/en not_active Ceased
- 1987-08-13 DE DE8787111720T patent/DE3766187D1/de not_active Expired - Lifetime
- 1987-08-13 AT AT87111720T patent/ATE58389T1/de not_active IP Right Cessation
- 1987-08-13 JP JP62504771A patent/JP2536889B2/ja not_active Expired - Lifetime
- 1987-08-13 BR BR8707772A patent/BR8707772A/pt not_active IP Right Cessation
- 1987-08-13 EP EP87905209A patent/EP0324741A1/de not_active Withdrawn
- 1987-08-13 ES ES87111720T patent/ES2018670B3/es not_active Expired - Lifetime
- 1987-08-13 EP EP87111720A patent/EP0256521B1/de not_active Expired - Lifetime
- 1987-08-13 NZ NZ221445A patent/NZ221445A/xx unknown
- 1987-08-13 WO PCT/EP1987/000445 patent/WO1988001287A1/de not_active Ceased
- 1987-08-13 RU SU874613521A patent/RU2074210C1/ru active
- 1987-08-14 CA CA000544527A patent/CA1306566C/en not_active Expired - Lifetime
- 1987-08-14 IE IE218287A patent/IE60579B1/en not_active IP Right Cessation
- 1987-08-14 PT PT85541A patent/PT85541B/pt unknown
- 1987-08-14 ZA ZA876028A patent/ZA876028B/xx unknown
- 1987-08-15 CN CN87106405A patent/CN1012069B/zh not_active Expired
-
1988
- 1988-04-13 NO NO881601A patent/NO300811B1/no unknown
- 1988-04-14 DK DK198802046A patent/DK172740B1/da not_active IP Right Cessation
-
1989
- 1989-02-15 FI FI890718A patent/FI97065C/fi not_active IP Right Cessation
-
1990
- 1990-12-21 GR GR90401123T patent/GR3002551T3/el unknown
-
1991
- 1991-01-08 US US07/642,243 patent/US5114993A/en not_active Expired - Fee Related
-
1993
- 1993-05-06 LT LTIP527A patent/LT3311B/lt not_active IP Right Cessation
- 1993-05-27 LV LVP-93-431A patent/LV10473B/lv unknown
- 1993-12-22 MD MD94-0049A patent/MD940049A/ro not_active Application Discontinuation
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3862914A (en) | 1972-11-01 | 1975-01-28 | Mobil Oil Corp | Water-based coatings from polyepoxides and polycarboxylic acid monoanhydrides |
| US4247439A (en) | 1973-11-06 | 1981-01-27 | E. I. Du Pont De Nemours And Company | Water-borne coating composition made from epoxy resin, polymeric acid and tertiary amine |
| US3960795A (en) | 1974-08-13 | 1976-06-01 | Ppg Industries, Inc. | Hydrolyzed reaction product of a polyepoxide with a phenolic compound having a group hydrolyzable to carboxyl |
| US4308185A (en) | 1976-05-11 | 1981-12-29 | Scm Corporation | Graft polymer compositions of terminated epoxy resin, processes for making and using same, and substrates coated therewith |
| US4212781A (en) | 1977-04-18 | 1980-07-15 | Scm Corporation | Modified epoxy resins, processes for making and using same and substrates coated therewith |
| EP0006334A1 (de) | 1978-06-12 | 1980-01-09 | Mobil Oil Corporation | Verfahren zur Herstellung von selbstemulgierbaren Epoxyharzester-Copolymeren und die so hergestellten Produkte |
| EP0006336A1 (de) | 1978-06-12 | 1980-01-09 | Mobil Oil Corporation | Überzugsmittel aus wässrigen Emulsionen auf der Basis von selbstemulgierbaren veresterten Polyepoxyden-Copolymeren Zusammensetzungen |
| DE3446178A1 (de) | 1983-12-21 | 1985-07-04 | Inmont Corp., Clifton, N.J. | Wasserverduennbare anstrichzusammensetzung, verfahren zu ihrer herstellung und ihre verwendung zum beschichten von behaeltern fuer nahrungsmittel |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| LT3311B (en) | Aqueous coating composition and process for manufacture thereof | |
| US10280332B2 (en) | Phosphatized polyesters and coating compositions containing the same | |
| AU2012258930A1 (en) | Phosphatized polyesters and coating compositions containing the same | |
| SG195022A1 (en) | Coating compositions with improved adhesion to containers | |
| JPS62240370A (ja) | コ−テイング法および熱硬化性水性塗料 | |
| US9321935B2 (en) | Container coating compositions | |
| US4303488A (en) | Electrocoating with water-borne coating composition made from epoxy resin, polymeric acid and tertiary amine | |
| US4740566A (en) | High gloss color keyed guide coat | |
| US5322863A (en) | Coating compound, process for its production as well as use thereof | |
| AU2014281601B2 (en) | Container coating compositions | |
| JPH09286951A (ja) | 缶外面塗料用樹脂組成物 | |
| NZ618116B2 (en) | Phosphatized polyesters and coating compositions containing the same | |
| JPH01229076A (ja) | 高光沢をもつ色調付与プライマー−サーフエーサー組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| TK9A | Rectifications: patents |
Free format text: C09D 163/02, C08L 63/00, 19960616, |
|
| MM9A | Lapsed patents |
Effective date: 19970506 |